Latest Articles

Subject

Article
Complete callosal agenesis, pontocerebellar hypoplasia, and axonal neuropathy due to AMPD2 loss
Ashley P.L. Marsh, Vesna Lukic, Kate Pope, et al.

July 16, 2015
Editorial
Are migraineurs naturally born “well-hearted”?
Anne Ducros

July 02, 2015
Editor's Note
Spotlight on the June 2015 issue
Stefan M. Pulst

July 02, 2015
Article
Genetic analysis for a shared biological basis between migraine and coronary artery disease
Bendik S. Winsvold, Christopher P. Nelson, Rainer Malik, et al.

July 02, 2015
Clinical/Scientific Notes
Loss-of-function mutations in RAB39B are associated with typical early-onset Parkinson disease
Suzanne Lesage, Jose Bras, Florence Cormier-Dequaire, et al.

June 18, 2015
Article
PFKM gene defect and glycogen storage disease GSDVII with misleading enzyme histochemistry
Mari Auranen, Johanna Palmio, Emil Ylikallio, et al.

June 04, 2015
Article
Epilepsy with auditory featuresA heterogeneous clinico-molecular disease
Tommaso Pippucci, Laura Licchetta, Sara Baldassari, et al.

May 14, 2015
Article
Respiratory chain deficiency in nonmitochondrial disease
Angela Pyle, Helen J. Nightingale, Helen Griffin, et al.

April 27, 2015
The Helix
Welcome to Neurology: Genetics
Stefan M. Pulst

April 17, 2015
Article
Epileptic encephalopathy-causing mutations in DNM1 impair synaptic vesicle endocytosis
Ryan S. Dhindsa, Shelton S. Bradrick, Xiaodi Yao, et al.

April 17, 2015

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